TY - JOUR
T1 - Isolation and Characterization of Nanobodies against a Zinc-Transporting P-Type ATPase
AU - Longhin, Elena
AU - Gronberg, Christina
AU - Hu, Qiaoxia
AU - Duelli, Annette Susanne
AU - Andersen, Kasper Rojkjaer
AU - Laursen, Nick Stub
AU - Gourdon, Pontus
PY - 2018
Y1 - 2018
N2 - P-type ATPases form a large and ubiquitous superfamily of ion and lipid transporters that use ATP (adenosine triphosphate) to carry out their function. The IB subclass (P-IB-ATPases) allows flux of heavy metals and are key players in metal detoxification, critical for human health, crops, and survival of pathogens. Nevertheless, P-IB-ATPases remain poorly understood at a molecular level. In this study, nanobodies (Nbs) are selected against the zinc-transporting P-IB-ATPase ZntA from Shigella sonnei (SsZntA), aiming at developing tools to assist the characterization of the structure and function of this class of transporters. We identify six different Nbs that bind detergent stabilized SsZntA. We further assess the effect of the Nbs on the catalytic function of SsZntA, and find that five nanobodies associate without affecting the function, while one nanobody significantly reduces the ATPase activity. This study paves the way for more refined mechanistical and structural studies of zinc-transporting P-IB-ATPases.
AB - P-type ATPases form a large and ubiquitous superfamily of ion and lipid transporters that use ATP (adenosine triphosphate) to carry out their function. The IB subclass (P-IB-ATPases) allows flux of heavy metals and are key players in metal detoxification, critical for human health, crops, and survival of pathogens. Nevertheless, P-IB-ATPases remain poorly understood at a molecular level. In this study, nanobodies (Nbs) are selected against the zinc-transporting P-IB-ATPase ZntA from Shigella sonnei (SsZntA), aiming at developing tools to assist the characterization of the structure and function of this class of transporters. We identify six different Nbs that bind detergent stabilized SsZntA. We further assess the effect of the Nbs on the catalytic function of SsZntA, and find that five nanobodies associate without affecting the function, while one nanobody significantly reduces the ATPase activity. This study paves the way for more refined mechanistical and structural studies of zinc-transporting P-IB-ATPases.
KW - P-type ATPase
KW - nanobody
KW - llama
KW - Zinc-transport
KW - Zinc-transporting P-ATPase
KW - ZntA
U2 - 10.3390/antib7040039
DO - 10.3390/antib7040039
M3 - Journal article
C2 - 31544889
VL - 7
JO - Antibodies
JF - Antibodies
SN - 2073-4468
IS - 4
M1 - 39
ER -